Evidence map›Paper›PMID 17049691›Full record

ArticleVaccine2007

Antibodies against trimeric S glycoprotein protect hamsters against SARS-CoV challenge despite their capacity to mediate FcgammaRII-dependent entry into B cells in vitro.

Yiu Wing Kam, François Kien, Anjeanette Roberts, Yan Chung Cheung, Elaine W Lamirande, Leatrice Vogel, Shui Ling Chu, Jane Tse, Jeannette Guarner, Sherif R Zaki and 4 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Vaccine, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04934111 (A Clinical Trial to Assess the Safety and Immunogenicity of LNP-nCOV saRNA-02, a Self-amplifying Ribonucleic Acid), which is not on this map. Cited by 146 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
146citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04934111 phase1unknown statusnot on this mapstarted 2021, after this paper: background citation

A Clinical Trial to Assess the Safety and Immunogenicity of LNP-nCOV saRNA-02, a Self-amplifying Ribonucleic Acid (saRNA) Vaccine, in SARS-CoV-2 Seronegative and Seropositive Uganda Population

TypeinterventionalSponsorMRC/UVRI and LSHTM Uganda Research UnitRan2021 to 2022Enrolled42ConditionsCOVID-19ArmsLNP-nCOV saRNA-02 Vaccine
3 · Its place in the literature

Who cites it

146 citing papers in PubMed, 1 synthesis or guideline pooled it, 220 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Antibody-dependent enhancement of coronaviruses.International journal of biological sciences · 2025
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Severe COVID-19: Drugs and Clinical Trials.Journal of clinical medicine · 2023
    Review
  9. Review
  10. Review
  11. Multifaceted roles of Fcγ receptors in COVID-19 and vaccine responses.American journal of translational research · 2023
    Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review

86 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 3 countries.

Yiu Wing KamHKU-Pasteur Research Centre, 8 Sassoon Road, Hong Kong SAR, China. Jasonkamyiuwing@yahoo.com.hk
François Kien
Anjeanette Roberts
Yan Chung Cheung
Elaine W Lamirande
Leatrice Vogel
Shui Ling Chu
Jane Tse
Jeannette Guarner
Sherif R Zaki
Kanta Subbarao
Malik Peiris
Béatrice Nal
Ralf Altmeyer
National Institutes of Health · USUniversity of Hong Kong · HKCenters for Disease Control and Prevention · USHKU-Pasteur Research Pole · HKChinese University of Hong Kong · CN

Funding

Vaccines, Immunoprophylaxis, and Immunotherapy for SARSZ01AI000934 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI SUBBARAO, KANTA · 2003 to 2008
$1.9M
INFLUENZA PANDEMIC PREPAREDNESS IN ASIA-N01AI095357 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · 1999 to 2003
$0k
NIAID NIH HHS AI95357
6 · The paper itself

Abstract

Vaccine-induced antibodies can prevent or, in the case of feline infectious peritonitis virus, aggravate infections by coronaviruses. We investigated whether a recombinant native full-length S-protein trimer (triSpike) of severe acute respiratory syndrome coronavirus (SARS-CoV) was able to elicit a neutralizing and protective immune response in animals and analyzed the capacity of anti-S antibodies to mediate antibody-dependent enhancement (ADE) of virus entry in vitro and enhancement of replication in vivo. SARS-CoV-specific serum and mucosal immunoglobulins were readily detected in immunized animals. Serum IgG blocked binding of the S-protein to the ACE2 receptor and neutralized SARS-CoV infection in vitro. Entry into human B cell lines occurred in a FcgammaRII-dependent and ACE2-independent fashion indicating that ADE of virus entry is a novel cell entry mechanism of SARS-CoV. Vaccinated animals showed no signs of enhanced lung pathology or hepatitis and viral load was undetectable or greatly reduced in lungs following challenge with SARS-CoV. Altogether our results indicate that a recombinant trimeric S protein was able to elicit an efficacious protective immune response in vivo and warrant concern in the safety evaluation of a human vaccine against SARS-CoV.

Indexed as

AnimalsAntibodies, ViralB-LymphocytesCricetinaeDose-Response Relationship, DrugImmunity, MucosalImmunoglobulin AImmunoglobulin GMembrane GlycoproteinsMiceReceptors, IgGSevere Acute Respiratory SyndromeSevere acute respiratory syndrome-related coronavirusSpike Glycoprotein, CoronavirusViral Envelope ProteinsAntibodies, ViralImmunoglobulin AImmunoglobulin GMembrane GlycoproteinsReceptors, IgGSpike Glycoprotein, Coronavirusspike glycoprotein, SARS-CoVspike protein, mouse hepatitis virusViral Envelope Proteins

Identifiers

PMID17049691
PMCPMC7115629
OpenAlexW2115343997

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.